Interrupted Aortic Arch Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Non-continuity of the arch of aorta with an atretic point or absent segment. (Human Phenotype Ontology, HP_0011611)
External Link https://www.disgenet.org/browser/0/1/0/C0152419
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Genes

12 genes associated with the disease Interrupted Aortic Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CFD complement factor D (adipsin)
CHD7 chromodomain helicase DNA binding protein 7
DIS3L2 DIS3 like 3'-5' exoribonuclease 2
FGFR1 fibroblast growth factor receptor 1
FOXC2 forkhead box C2
GATA6 GATA binding protein 6
HOXA1 homeobox A1
KRAS Kirsten rat sarcoma viral oncogene homolog
MMP21 matrix metallopeptidase 21
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SMG9 SMG9 nonsense mediated mRNA decay factor
TBX1 T-box 1